A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550036



Internal ID20923188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151020876..151022360hg38UCSC Ensembl
chr1:150993352..150994836hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381485
hg191485
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248130
Samples
Known GenesPRUNE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550036
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer